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rs869312968

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312968(A;G)
Make rs869312968(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position6023301
GeneAIMP2, EIF2AK1
is asnp
is mentioned by
dbSNPrs869312968
ebirs869312968
HLIrs869312968
Exacrs869312968
Varsomers869312968
Maprs869312968
PheGenIrs869312968
hapmaprs869312968
1000 genomesrs869312968
hgdprs869312968
ensemblrs869312968
gopubmedrs869312968
geneviewrs869312968
scholarrs869312968
googlers869312968
pharmgkbrs869312968
gwascentralrs869312968
openSNPrs869312968
23andMers869312968
23andMe allrs869312968
SNP Nexus

SNPshotrs869312968
SNPdbers869312968
MSV3drs869312968
GWAS Ctlgrs869312968
Max Magnitude0
ClinVar
Risk rs869312968(G;G)
Alt rs869312968(G;G)
Reference rs869312968(A;A)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene AIMP2 EIF2AK1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000007.13:g.6062932A>G
CLNSRC
CLNACC RCV000210704.1,